تفاعل #65748

ord-80287ea4dd174b418b35ca7cef4f89ef

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىas obtained in Reference Example 18
  2. 2
    workup.DISTILLATIONthe solvent was distilled off
  3. 3
    workup.ADDITIONWater was added to the residue
  4. 4
    استخلاصthe mixture was extracted with ethyl acetate
  5. 5
    غسيلThe organic layer was washed with water
  6. 6
    تجفيفa saturated aqueous solution of sodium chloride and dried
  7. 7
    workup.DISTILLATIONThe solvent was distilled off
  8. 8
    أخرىThe residue was purified by silica gel column chromatography (eluent:ethyl acetate)
  9. 9
    ترشيحThe resulting crystals were collected by filtration with hexane

الإجراء التجريبي

In 25 ml of methanol was dissolved 1.2 g of 2-chloro-3,4-diethoxycarbonyl-5-nitro-6-phenylpyridine as obtained in Reference Example 18. To the solution was added 6.34 ml (2.0 eq.) of a solution of 1N sodium methoxide in methanol, and the mixture was stirred at room temperature for 30 minutes. The reaction mixture was neutralized with 0.2 ml (1.1 eq.) of acetic acid, and the solvent was distilled off. Water was added to the residue, and the mixture was extracted with ethyl acetate. The organic layer was washed with water and a saturated aqueous solution of sodium chloride and dried. The solvent was distilled off. The residue was purified by silica gel column chromatography (eluent:ethyl acetate). The resulting crystals were collected by filtration with hexane.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05420275uspto-grants-1995_05